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About Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas, including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral, and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 people across 40+ countries.

Position Name :

Drug Safety Specialist

Organization :



B.Pharm, M.Pharm, Bsc, Msc, Pharm.D, Lifesciences, Nursing


1 Year


₹3L – ₹7L/yr


Navi Mumbai

We are seeking a full-time, office-based Clinical Safety Coordinator to join our Clinical Safety department in India. This position involves handling and processing adverse events from all sources, including clinical trials and post-marketing surveillance. This role offers a fantastic opportunity to use your previous expertise and further develop your career.


  • Develop action plans for incoming safety-related calls.
  • Collect, process, and track adverse and serious adverse events.
  • Write detailed safety narratives.
  • Report various safety data.
  • Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.


  • Bachelor’s degree in a healthcare-related field such as Nursing, Pharmacy, or Pharmacology.
  • Preferred: Clinical experience or experience in Clinical Research, case processing, and Post-Marketing Pharmacovigilance.
  • Proficient in English.
  • Strong knowledge of Microsoft® Office.
  • Broad knowledge of medical terminology.
  • Strong organizational and communication skills.

Application Link

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